首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >Arginine-rich RNA binding domain and protein scaffold domain of RNase E are important for degradation of RNAI but not for that of the Rep mRNA of the ColE2 plasmid.
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Arginine-rich RNA binding domain and protein scaffold domain of RNase E are important for degradation of RNAI but not for that of the Rep mRNA of the ColE2 plasmid.

机译:RNase E的富含精氨酸的RNA结合结构域和蛋白质支架结构域对RNAI的降解很重要,但对ColE2质粒的Rep mRNA的降解却不重要。

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摘要

Expression of the replication initiator protein (Rep) of the ColE2 plasmid is controlled by antisense RNA (RNAI). Therefore alterations in processes and/or rates of degradation of these two RNAs would affect the Rep expression. Here, we have shown that the arginine-rich RNA binding domain (ARRBD) of RNase E is important for the initial endoribonucleolytic cleavage of RNAI but dispensable for the endoribonucleolytic cleavages of the Rep mRNA. We have also shown that the protein scaffold domain of RNase E is important for successive exoribonucleolytic degradation of RNAI, suggesting involvement of RhlB, but dispensable for that of the Rep mRNA. Such differences in the initiation and successive steps of degradation between RNAI and the Rep mRNA might be important in determining their individual degradation efficiencies required for a quick response to the changes in the plasmid copy number.
机译:ColE2质粒的复制起始蛋白(Rep)的表达受反义RNA(RNAI)的控制。因此,这两个RNA的过程和/或降解速率的改变将影响Rep表达。在这里,我们已经显示,RNase E的富含精氨酸的RNA结合结构域(ARRBD)对于RNAI的初始核糖核酸内切酶裂解很重要,但对于Rep mRNA的核糖核酸内切酶裂解是必不可少的。我们还表明,RNase E的蛋白质支架结构域对于连续的核糖核酸外切核糖核酸降解至关重要,提示RhlB参与其中,但对于Rep mRNA却是必不可少的。 RNAI和Rep mRNA之间的降解起始步骤和后续降解步骤之间的这种差异可能对确定对质粒拷贝数变化的快速响应所需的它们各自的降解效率很重要。

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